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Completed

NCT Number: NCT05459389

Early Targeted Antibiotic Therapy in Patients With Sepsis

The aim of this study is to assess the efficacy of early targeted antibiotic therapy in patients with sepsis and septic shock using the new biomarker Sirtuin 1 and PCR for bacterial resistance detection.

The primary outcome is change in SOFA score (ΔSOFA) which will be calculated by subtracting the final SOFA score and sirtuin 1 level at 5 days from the corresponding initial value at enrollment.

Secondary outcomes included mortality rates, ventilator free days and length of icu stay.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rehab Hussein Werida

Damanhūr, Elbehairah, 31527, Egypt

About this study

  • A prospective, single-center, open labeled, randomized interventional study
  • Patients will be recruited from a private hospital in Alexandria
  • Approval will be obtained from Research Ethics Committee of Faculty of Pharmacy, Damanhour University
  • Fourty eight critically ill patients, with sepsis and septic shock according to the 2016 third international consensus definitions, will be included
  • Patients with risk for Carbapenemase producing organisms:
  • Use of broad spectrum cephalosporins and/or carbapenems within the past three months
  • Polytrauma
  • Diabetes
  • Malignancy
  • Organ transplantation
  • Mechanical ventilation
  • Indwelling urinary or venous catheters
  • Overall poor functional status or severe illness
  • Residence in a long-term care facility(18-28).
  • The baseline characteristics of the patients will be collected at the time of enrollment. The collected data included age, sex, ratio of septic shock to sepsis, ratio of ventilated to non-ventilated patients, source of infection, vital signs, laboratory data, arterial blood gas (ABG), APACHE II score, Glasgow Coma Scale score, and SOFA scores. The level of Procalcitonin (PCT) and Sirtuin-1 will also be measured at this time(29).
  • Patients will be randomly allocated to antibiotic regimen guided by conventional culture technique (n=24) or targeted antibiotics therapy guided by resistance genotyping (n=24) (29, 30).
  • Levels of Sirtuin1 will be detected using ELISA kits as prescribed by manufacturer.
  • Traditional diagnostic microbiology techniques relying on the growth of organisms on appropriate culture media (Control group).
  • Qualitative Multiplex pcr test will be used for rapid detection of carbapenemases genes (Intervention group)
  • Statistical tests appropriate to the study will be conducted to evaluate significance of results
  • Results, conclusion, discussion and recommendations will be given.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female patients 18 years or older
  • A definite diagnosis of sepsis or septic shock according to the definition of the 2016 SCCM/ESICM task force.
  • Patients at risk for carbapenemase producing organisms

Exclusion criteria

  • Pregnant and lactating women
  • hematological disorders (e.g., leukemia, myelodysplastic syndrome, neoplastic metastases to bone marrow),
  • life-threatening diseases (e.g., malignant solid tumors), acquired immunodeficiency syndrome.
  • Lethal traumatic injury
  • Acute Physiologic Assessment and Chronic Health Evaluation II (APACHE II) score ≥34 (due to high predicted mortality of 80%)
  • Primary fungal or viral infections

Treatment and study plan

targeted antibiotics therapy

Other

targeted antibiotics therapy guided by resistance genotyping (n=24)

Other names: genotyping

Primary outcomes

  1. Sirtuin1 (ng/ml)

    Time frame: 5 days

    Levels of Sirtuin1 will be detected using ELISA kits as prescribed by manufacturer.

  2. SOFA (score)

    Time frame: 5 days

    SOFA score (ΔSOFA) which will be calculated by subtracting the final SOFA score at 5 days from the corresponding initial value at enrollment.

Secondary outcomes

  1. mortality rates (%)

    Time frame: 5 days

    number of dead patients.

  2. ventilator free days (days)

    Time frame: 5 days

    count of days free from ventilator,

  3. length of icu stay (Days)

    Time frame: 5 days

    count of days in ICU

Sponsors and collaborators

Lead sponsor

Rehab Werida

Other

Registry information

Official study title

Efficacy of Early Targeted Antibiotic Therapy in Patients With Sepsis and Septic Shock

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Jul 15, 2022
Registry last updated
Sep 28, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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